NM_004629.2(FANCG):c.592C>T (p.Gln198Ter) AND Fanconi anemia complementation group G
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Feb 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003461501.1
Allele description [Variation Report for NM_004629.2(FANCG):c.592C>T (p.Gln198Ter)]
NM_004629.2(FANCG):c.592C>T (p.Gln198Ter)
Condition(s)
Assertion and evidence details
Last Updated: Dec 30, 2023